rs61755792 has not been reported to ClinVar. Refer to dbSNP record rs61755792 for details on variation at this location. Please consider submitting your interpretation of this variant to ClinVar
Genetic variation
- Clinical significance: not reported in ClinVar
- Reference allele: G
- Variation alleles: A, C, T
- Variation type: single nucleotide variation
- Organism: Homo sapiens
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GRCh38.p14: NC_000006.12: 42,721,820
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GRCh37.p13: NC_000006.11: 42,689,558
Genome Data Viewer
Source: KnownItemSensor
| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Cone-rod dystrophy +9 more | GPathogenic/Likely pathogenic |
Click to view in NCBI Gene